B. M. R. Harvey
Queen's University Belfast
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Featured researches published by B. M. R. Harvey.
Planta | 1969
David M. Reid; Alan Crozier; B. M. R. Harvey
SummaryGibberellin (GA)-like substances are shown to be present in the bleeding sap of tomatoes. It is demonstrated that these substances can promote stem elongation in intact tomato plants. Waterlogging of the root system inhibits stem growth and severely reduces the export of GAs from the root to the shoot in the xylem sap. It is suggested that decline in growth rate following waterlogging may, in part, be due to the reduction in the supply of GAs to the shoot.
Plant Cell Tissue and Organ Culture | 1991
B. M. R. Harvey; Samuel H. Crothers; Nicola E. Evans; C. Selby
The growth retardant chlormequat stimulated microtuber formation by a recalcitrant cultivar of potato (Solanum tuberosum), but reduced microtuber fresh weight in a cultivar that tuberised readily in its absence. Inhibition of microtuber growth by high concentrations of chlormequat was confirmed using a different in vitro system where all cultivars tuberised in the absence of growth retardants.Alternative growth retardants were tested. Daminozide also had a detrimental effect on microtuber fresh weight, but ancymidol and paclobutrazol did not inhibit microtuber growth at the concentrations required for stimulation of tuberisation by recalcitrant cultivars. In addition, 10-5 M ancymidol and paclobutrazol inhibited premature sprouting of microtubers in vitro.
Plant Growth Regulation | 1996
Ffiona V. M. Richardson; Seán Mac An tSaoir; B. M. R. Harvey
Light microscopy was used to study graft union formation in in vitro micrografts of tissue cultured apple (Malus domestica. Borkh). Micrografts were constructed using horizontal incisions to form the grafting surface, and placing the cut ends of rootstock and scion into sterile silicon tubing to permit graft formation to occur.The outer morphological and histological development was similar for different stock-scion micrograft combinations but graft union formation was slower in heterografts than in autografts. Initial leaf expansion at the scion shoot apex occurred in all micrografted plantlets within 1–4 days and was not indicative of graft success. Progressive scion growth and development could be used as an indication of graft success by ten to fourteen days after grafting and probably was related to establisment of cell to cell contact at the graft interface. Microscopy showed initiation of callus proliferation in the vascular cumbium and the pith ten days after grafting. Differentiation was observed subsequently and this was reflected in scion development. Longitudinally orientated cambial cells began to differentiate between twenty and forty days after grafting, and formed a bridge between the vascular cylinders of scion and rootstock. The scions at this stage had as many as eight newly expanded leaves and micrografts were strong enough to permit silicon sleeve removal without damage. Continuity of new vascular elements in rootstock and scion was established around forty days. New vascular elements curved slightly in towards the pith to form a ‘c’ shaped bridge across the graft union. Vascular development continued until it reached completion after six months.
Potato Research | 1998
Fokion Papathanasiou; Samuel H Mitchell; B. M. R. Harvey
SummaryPlants of early potato cultivars were sampled at successive harvests during tuber development and individual tubers were analysed for α-solanine and α-chaconine using high-performance liquid chromatography. Mean tuber total glycoalkaloid concentration (α-solanine plus α-chaconine) per plant decreased with time and statistically significant differences between cultivars were observed in the patterns of decline during tuber growth. The mean tuber ratio of α-chaconine to α-solanine increased during tuber development and was also affected by genotype. Total glycoalkaloid concentration for individual tubers of marketable sizes (up to 50 g fresh weight) exceeded the safety limit of 20 mg per 100 g fresh weight for cultivars Home Guard and British Queen but not for Rocket. These differences were attributable to differences in both rates and patterns of glycoalkaloid accumulation during tuber development, although in all cultivars results were consistent with glycoalkaloid accumulation occurring in the expanding peripheral cell layers of tubers for a considerable period after tuber initiation.
Plant Cell Tissue and Organ Culture | 2005
Ioanna Staikidou; Sally Watson; B. M. R. Harvey; C. Selby
Shoot clump cultures of Narcissus cultivars St. Keverne and Hawera were used to investigate the effects of culture medium carbon supply, type of carbohydrate and osmolarity on in vitro bulblet development. Increasing the medium osmolarity using mannitol or sorbitol, which did not act as substrates for growth, failed to stimulate bulblet formation with either cultivar. An exception to this was a relatively small increase in total bulblet dry weight per culture, in the cultivar Hawera only, caused by adding 30 g l −1 sorbitol in combination with 30 g l−1 sucrose. Simultaneously increasing the medium osmolarity and carbon supply using the metabolisable carbohydrate sources, sucrose, glucose, fructose or an equimolar mixture of glucose and fructose stimulated bulblet production, total dry matter accumulation and partitioning into bulblets. At comparable levels of carbon supply up to 19.0 g l−1, bulblet development of both cultivars was similar with monosaccharide and sucrose media. This indicates that substrate supply is more important for bulblet development than osmolarity of the culture medium. The cultivar Hawera also showed similar responses to monosaccharide and sucrose media supplying 37.9 g C l−1, despite the high osmolarity of monosaccharide media (c. 650 m Osm kg−1, equivalent to −1.6 MPa, compared to 380 m Osm kg−1 for sucrose medium). However in St. Keverne total dry matter accumulation and dry weight per bulblet were further stimulated only by increasing the sucrose supply from 19.0 to 37.9 g C l−1, not by increasing the monosaccharide supply. Implications of the findings for Narcissus micropropagation are discussed.
Plant Cell Tissue and Organ Culture | 1992
Y. N. Chow; C. Selby; B. M. R. Harvey
AbstractA simple method for stimulating and maintaining high in vitro multiplication of Narcissus shoot clump cultures was developed. Shoot clumps were subjected either to ‘normal cutting’ where leaves were trimmed to 20 mm in length at the beginning of each culture passage or to ‘severe cutting’ where shoot clumps were cut down to the basal plate region removing all green tissue. ‘Severe cutting’ at the beginning of each culture passage initially doubled the leaf multiplication, compared to ‘normal cutting’, but the difference between cutting treatments declined in successive passages. The improvement in leaf multiplication was maintained when shoot clumps were subjected to ‘severe cutting’ only at every other culture passage, with no cutting in the alternate ‘recovery’ passages. In vitro multiplication was increased by ‘severe cutting’ in all seven Narcissus cultivars which were tested.
Journal of the Science of Food and Agriculture | 1999
Fokion Papathanasiou; Samuel H Mitchell; Sally Watson; B. M. R. Harvey
The effects of low temperature and of combined stresses, cool temperature and waterlogging and also warm temperature and drought, on potato tuber glycoalkaloid levels were investigated, with emphasis on comparison of tubers of similar size. The early maturing cultivars Home Guard, Rocket and British Queen were grown under favourable controlled environment conditions (18/14 °C day/night temperature, 14h photoperiod) until the imposition of treatments after the start of tuber initiation. Transfer to low temperature (12/9 °C) did not increase total glycoalkaloid concentration in any of the three cultivars. However, waterlogging at 12/9 °C increased total glycoalkaloid concentration during the later stages of development of British Queen. Drought stress at 24/18 °C also increased total glycoalkaloid concentration in British Queen, although the response varied between individual tubers of similar size. Total glycoalkaloid concentrations in tubers of Rocket were not affected by the combined stress treatments, and any effects on Home Guard were very much less than on British Queen. # 1999 Society of Chemical Industry
Journal of the Science of Food and Agriculture | 1999
Fokion Papathanasiou; Samuel H Mitchell; B. M. R. Harvey
Individual tubers from mature plants of cultivars Pentland Dell and Estima were harvested from experimental plots in two successive years and analysed for α-solanine, α-chaconine and total glycoalkaloid concentration (α-solanine and α-chaconine combined) using high-performance liquid chromatography. Mean tuber glycoalkaloid concentration per plant was strongly affected by genotype and was much higher in plants of Pentland Dell (10.0 and 16.3 mg per 100 g fresh weight in 1994 and 1995, respectively) than Estima (4.0 and 4.3 mg per 100 g fresh weight in 1994 and 1995, respectively). The variation between plants in mean tuber glycoalkaloid concentration, expressed as coefficient of variation, was similar for the two cultivars in both years. Variation within plants was higher for cultivar Pentland Dell than Estima for both years but it was statistically significant only in 1995. Tuber position within a plant had no effect on glycoalkaloid concentrations in tubers of similar size. An inverse relationship between total glycoalkaloid concentration and tuber fresh weight of individual tubers was found for both cultivars and small tubers of Pentland Dell (20–40 g fresh weight) exceeded the safety limit of 20 mg per 100 g fresh weight. The pattern of glycoalkaloid accumulation differed between genotypes and appeared related to tuber growth. The implications of these results in terms of food safety are discussed. © 1999 Society of Chemical Industry
Plant Growth Regulation | 1996
Chris Selby; W. Colin McRoberts; John T. G. Hamilton; B. M. R. Harvey
The maturation of somatic embryos of Sitka spruce [Picea sitchensis (Bong.) Carr.] was found to be highly dependent on the method used to seal plastic Petri dishes. Large numbers of well-formed mature embryos developed if dishes were sealed with PVC cling-film (CF) whilst sealing with Parafilm M (PF) greatly reduced the numbers of embryos forming. Inclusion of potassium permanganate oxidation traps, normally used to deplete the atmospheric ethylene, greatly stimulated somatic embryo maturation under PF sealing. Similarly, traps of adsorption agents (Tenax, activated charcoal or soft white paraffin), capable of removing volatiles from the culture vessel head-space, stimulated somatic embryo maturation under PF sealing although to a lesser extent than the oxidation traps. Incorporation of silver nitrate or 2-chloroethylphosphonic acid (ethephon) in the culture medium indicated that ethylene was not the agent supressing somatic embryo maturation under PF sealing.
Potato Research | 1992
B. M. R. Harvey; S. H. Crothers; S. Watson; H. C. Lee
SummaryMicrotuber formation by single node stem segments of in vitro grown potato plantlets was used as a model system for investigation of heat inhibition of tuber development. The stem segments were incubated in darkness at 20°C or 26°C on a tuberisation medium containing benzyl aminopurine (140 μg 1−1) and sucrose (80 g 1−1). Continuous incubation at 26°C strongly inhibited tuberisation and exposure to 26°C for only 1 week before transfer to 20°C significantly reduced microtuber fresh weight. Inclusion of a gibberellin synthesis inhibitor, paclobutrazol (10−5 M), in the tuberisation medium counteracted the heat inhibition of tuber initiation but not the reduction of microtuber fresh weight. Thus, consistent with previous reports, inhibition of tuber initiation appears attributable to increased endogenous levels of gibberellins. Possible causes of the reduction in microtuber fresh weight are discussed.